While hereditary cancer syndromes have been described and studied for centuries, the
completion of the human genome project fueled accelerated progress in precision medicine …

OBJECTIVE: To examine user uptake and experience with a clinical chatbot that automates
hereditary cancer risk triage by collecting personal and family cancer history in routine …

Since the completion of the Human Genome Project, considerable progress has been made
in translating knowledge about the genetic basis of disease risk and treatment response into …

Obesity, diabetes and cardiovascular events are non-communicable diseases (NCDs)
directly related to lifestyle and life quality. Rises on NCDs rates are leading to increases in …

Primary care physicians (PCPs) are commonly approached with concerns involving patient
genetics. This is a challenge because most PCPs lack expertise in genetic testing compared …

Importance Most patients with pathogenic or likely pathogenic (P/LP) variants for breast
cancer have not undergone genetic testing. Objective To identify patients meeting family …

A person's phenotypic sex (ie, endogenous expression of primary, secondary, and
endocrinological sex characteristics) can impact crucial aspects of genetic assessment and …

Abstract Information about the NMR metabolomics landscape of overall, and common
cancers is still limited. Based on a cohort of 83,290 participants from the UK Biobank, we …

Background Family history assessment can identify individuals above population-risk for
cancer to enable targeted Screening, Prevention, and Early Detection (SPED). Family …

Background As the incidence of gastric cancer increases sharply in adults aged over 45
years, a better understanding of gastric cancer screening knowledge and practice is crucial …